Suppliers / Bora Pharmaceutical Laboratories

Bora Pharmaceutical Laboratories

Taiwan Updated 9 July 2026

Bora Pharmaceutical Laboratories is a finished-dose manufacturer based in Taiwan. It appears in 2 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by MHRA (UK).

0
active US DMFs
0
valid CEPs
1
registered plants
2
filings across 1 regulators

Registered plants

Site FDA FEI
JHUNAN, Taiwan Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NPRA (MY) 2 None
MHRA (UK) None 1

Questions about Bora Pharmaceutical Laboratories

Does Bora Pharmaceutical Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Bora Pharmaceutical Laboratories. It does have 2 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Bora Pharmaceutical Laboratories manufacture?
1 registered site is on record, in Taiwan (Jhunan). Every site is listed on this page with the register it came from.
Which regulators recognise Bora Pharmaceutical Laboratories's GMP?
Current GMP certificates are on record from MHRA (UK). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates